ZMP
si:dkeyp-94b4.3
Ensembl ID:
Description:
Novel protein similar to H.sapiens phospholipase C, delta [Source:UniProtKB/TrEMBL;Acc:B8JIR0]
Human Orthologue:
PLCD3
Human Description:
phospholipase C, delta 3 [Source:HGNC Symbol;Acc:9061]
Mouse Orthologue:
Plcd3
Mouse Description:
phospholipase C, delta 3 Gene [Source:MGI Symbol;Acc:MGI:107451]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31867 | Essential Splice Site | Available for shipment | Available now |
sa22061 | Essential Splice Site | Available for shipment | Available now |
sa22062 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31867
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079784 | Essential Splice Site | 275 | 769 | 5 | 15 |
ENSDART00000135143 | Essential Splice Site | 120 | 244 | 2 | 5 |
ENSDART00000145612 | None | None | 287 | None | 6 |
ENSDART00000079784 | Essential Splice Site | 275 | 769 | 5 | 15 |
ENSDART00000135143 | Essential Splice Site | 120 | 244 | 2 | 5 |
ENSDART00000145612 | None | None | 287 | None | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 16483774)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 15594739 |
GRCz11 | 12 | 15637046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGTACATGCGCAGAGCCTCATCCTCACCTATGAGCTCAATGAATGGGG[T/A]ATCTTCTATTCACTTTTTGTGTTTTTTTGTATACACAATTCTTGGTAGAA
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATATATAAAGCAATAATATAAAAAATAGATAATATAAAATAATACATGTCTAAACAGATCAACTATACAAATTAATTTAACATTGAATAAAAGCATGAACACTTAAGAACAAATGCATATATACAGTGTATAGACAGTTTTGAACTGCTATTTATATTGTTATGAAAAGTATTTTTCTTGATGTTAAATTTCAATTCTGTAATCTGCTTTAAATGTCTTTGTGCATTAGAAAAGTGATAAATCAGCAGATGGACGGCTTGAACATGAGGAGATCGAGCTATTTTGCCGTGAGTTGCTACGTCGGCCAGAGTTGGATGCAGTGTTTCAACAGTACTCTGCAAACGGTTGTGTCCTGTCCACTGTGGATTTGCGGGAATTCCTGAAAGATCAGGGCGAGGACCACACCCTTGTACATGCGCAGAGCCTCATCCTCACCTATGAGCTCAATGAATGGGG[T/A]ATCTTCTATTCACTTTTTGTGTTTTTTTGTATACACAATTCTTGGTAGAAACACTCCAGATCAGTGATGCCCAAGCTATGGCCCATGGTAACCTTTAATTTGGCCCGCCATCCCTTCTAAGAAGAGTGGGAGAATCATGGTTGAGATTTTCAATTCGAATTTCATGTAATATAGCACGTTGTTTGTTTTATTGTTAAATGCTAACTGAAATTAAATGTTTTAATTATATGGCTTAAATTAACCAGATTTTGTTTAAATGTATATTCTGTCATCTGACAATGCAGAGACTTTGAAGTGCAAGTCAAGTCAAATACAGATTCTCATTGTCCTGTGAATTTAACATTGAACTCTACTGTGTTATAAATATGCTTGTTTATGTTTTATAAATTATAATTTAAAAACTTATACTGCATTTTGAAATATAATGAAATAAAGTAGGAAATTACCCATGGCAAATTTAATGTAATCTAGATTGGTACATTAACTATCGGCCCACAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22061
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079784 | Essential Splice Site | 275 | 769 | 5 | 15 |
ENSDART00000135143 | Essential Splice Site | 120 | 244 | 2 | 5 |
ENSDART00000145612 | None | None | 287 | None | 6 |
ENSDART00000079784 | Essential Splice Site | 275 | 769 | 5 | 15 |
ENSDART00000135143 | Essential Splice Site | 120 | 244 | 2 | 5 |
ENSDART00000145612 | None | None | 287 | None | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 16483774)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 15594739 |
GRCz11 | 12 | 15637046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGTACATGCGCAGAGCCTCATCCTCACCTATGAGCTCAATGAATGGGG[T/A]ATCTTCTATTCACTTTTTGTGTTTTTTTGTATACACAATTCTTGGTAGAA
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATATATAAAGCAATAATATAAAAAATAGATAATATAAAATAATACATGTCTAAACAGATCAACTATACAAATTAATTTAACATTGAATAAAAGCATGAACACTTAAGAACAAATGCATATATACAGTGTATAGACAGTTTTGAACTGCTATTTATATTGTTATGAAAAGTATTTTTCTTGATGTTAAATTTCAATTCTGTAATCTGCTTTAAATGTCTTTGTGCATTAGAAAAGTGATAAATCAGCAGATGGACGGCTTGAACATGAGGAGATCGAGCTATTTTGCCGTGAGTTGCTACGTCGGCCAGAGTTGGATGCAGTGTTTCAACAGTACTCTGCAAACGGTTGTGTCCTGTCCACTGTGGATTTGCGGGAATTCCTGAAAGATCAGGGCGAGGACCACACCCTTGTACATGCGCAGAGCCTCATCCTCACCTATGAGCTCAATGAATGGGG[T/C]ATCTTCTATTCACTTTTTGTGTTTTTTTGTATACACAATTCTTGGTAGAAACACTCCAGATCAGTGATGCCCAAGCTATGGCCCATGGTAACCTTTAATTTGGCCCGCCATCCCTTCTAAGAAGAGTGGGAGAATCATGGTTGAGATTTTCAATTCGAATTTCATGTAATATAGCACGTTGTTTGTTTTATTGTTAAATGCTAACTGAAATTAAATGTTTTAATTATATGGCTTAAATTAACCAGATTTTGTTTAAATGTATATTCTGTCATCTGACAATGCAGAGACTTTGAAGTGCAAGTCAAGTCAAATACAGATTCTCATTGTCCTGTGAATTTAACATTGAACTCTACTGTGTTATAAATATGCTTGTTTATGTTTTATAAATTATAATTTAAAAACTTATACTGCATTTTGAAATATAATGAAATAAAGTAGGAAATTACCCATGGCAAATTTAATGTAATCTAGATTGGTACATTAACTATCGGCCCACAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22062
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079784 | Nonsense | 586 | 769 | 12 | 15 |
ENSDART00000135143 | None | None | 244 | None | 5 |
ENSDART00000145612 | Nonsense | 104 | 287 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 16505854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 15616819 |
GRCz11 | 12 | 15659126 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCAGTGGCACTGAACTTCCAAACCCAATCTGAAGAGATGGATCTGAAC[A/T]GAGGCCGTTTCTTAGCAAACGGAAATTGCGGCTATGTGCTAAAACCAAGC
Long Flanking Sequence:
GTTTAAACGACACACATGTAGGAGTTTTTCCATAATTTGGCAAAAAAGCACATAAATACCTTATGTATTCATGAGTGATATTAAAGTGATTTTGATTTGTTTTATTTCCTTTACATATTATTTTTCATATTTTAATAATGCTTTTGTTTCCAAAATTGCAATACAGTGAAGGCATTTTATGTCAAACGAATATTTATGTTTGTGGATGCCAATTTTTTTTTTTAATTTTCTTTGTGTGTGTCTAGGAAAACTGTTTGTACGTCACAACAGTGTTCAACTGAGCCGAATCTATCCATCTGGTCAGAGGGTGCAGTCTTCTAACTACAACCCTCAGGACATGTGGAATGCTGGTTGCCAGATAGGTAAACATTTATTGAAGAAAAATGTGCAGACCATGCAAAAATGTAAAAATGACAGTCCATATTTATAAATGACTGACAAAAAGCTATTTTGCAGTGGCACTGAACTTCCAAACCCAATCTGAAGAGATGGATCTGAAC[A/T]GAGGCCGTTTCTTAGCAAACGGAAATTGCGGCTATGTGCTAAAACCAAGCTTTATGTGCCAGCCTGATTCAGAGTTTAACCCAGAAAACACTGGGGGAGGTCCTGGCTACAACCCGACACTACTAACTATCAAGGTAAACCATCTAAACAGAGCAGTCTTTGTGAAAACAAAACCTCACATCTGCTGCCTCTCTATTTCCAGCTAGAACAAATTATTTGAAATACTGAAGTTGAGTGCCATAAAGTAAACACATTTGACCTGCAGATATATTTGGGAAAAATAGTCTAAAAATTTAAATGAATCAGTAAAATAGTGGCAGCCTCAATTTCCATGCAGTGTTTTAGAATACATTATCCAGCAAACAGTTTTGTGTTTAATAGATCAGCTTGGCTAAAACGAGGCTAAACTTGGGCTTTTATTGAAAATCTAATAGGCAACTAAGAATAGCCGAGAACTAGACTAGTCGTCAATTAGACAGATTAGACAGACTTTATATGTG
Associated Phenotype:
Not determined